NDC | 49967-618-01, 49967-618-02, 49967-618-03, 49967-618-04 |
Set ID | 09e7f362-6187-4e49-b703-8249c70e5124 |
Category | HUMAN OTC DRUG LABEL |
Packager | L'Oreal USA Products Inc |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333D |
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, coco-glucoside, propylene glycol, ammonium polyacryloyldimethyl taurate, glycerin, coco-betaine, sodium cocoyl isethionate, sodium methyl cocoyl taurate, dipropylene glycol, sodium chloride, butylene glycol, phenoxyethanol, sodium hydroxide, citric acid, hydrogenated coconut acid, capryloyl salicylic acid, coconut acid, sodium PCA, camphor, menthol, boswellia serrata resin extract, sodium isethionate, hamamelis virginiana (witch hazel) water, peumus boldus leaf extract, disodium EDTA, alcohol, zingiber officinale (ginger) root extract, sanguisorba officinalis root extract, cinnamomum cassia bark extract, xanthan gum
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KIEHLS SINCE 1851 BLUE HERBAL ACNE CLEANSER TREATMENT
salicylic acid lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-618 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 15 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCO GLUCOSIDE (UNII: ICS790225B) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) COCO-BETAINE (UNII: 03DH2IZ3FY) SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493) SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G) DIPROPYLENE GLYCOL (UNII: E107L85C40) SODIUM CHLORIDE (UNII: 451W47IQ8X) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM HYDROXIDE (UNII: 55X04QC32I) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM) CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4) COCONUT ACID (UNII: 40U37V505D) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) MENTHOL (UNII: L7T10EIP3A) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) SODIUM ISETHIONATE (UNII: 3R36J71C17) HAMAMELIS VIRGINIANA TOP WATER (UNII: NT00Y05A2V) PEUMUS BOLDUS LEAF (UNII: Q4EWM09M3O) EDETATE DISODIUM (UNII: 7FLD91C86K) ALCOHOL (UNII: 3K9958V90M) GINGER (UNII: C5529G5JPQ) SANGUISORBA OFFICINALIS ROOT (UNII: 4NYV2HT01X) CHINESE CINNAMON (UNII: WS4CQ062KM) XANTHAN GUM (UNII: TTV12P4NEE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-618-01 75 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2017 2 NDC:49967-618-02 150 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2017 3 NDC:49967-618-03 30 mL in 1 TUBE; Type 0: Not a Combination Product 03/01/2017 4 NDC:49967-618-04 3 mL in 1 PACKET; Type 0: Not a Combination Product 03/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333D 03/01/2017 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations L'Oreal USA, Inc. 185931458 manufacture(49967-618) , pack(49967-618)